Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g31960 | A05 | 34364951 | C | T | missense_variant | MODERATE | c.1699G>A|p.Gly567Arg |
S130 |
2 | BAA05g31960 | A05 | 34365497 | C | T | missense_variant | MODERATE | c.1222G>A|p.Ala408Thr |
S211 S227 |
3 | BAA05g31960 | A05 | 34366398 | G | A | missense_variant | MODERATE | c.800C>T|p.Ala267Val |
S219 |
4 | BAA05g31960 | A05 | 34366870 | G | A | missense_variant | MODERATE | c.472C>T|p.Pro158Ser |
S267 |
5 | BAA05g31960 | A05 | 34366974 | G | A | missense_variant | MODERATE | c.368C>T|p.Ser123Leu |
S217 S248 |
6 | BAA05g31960 | A05 | 34367370 | G | A | synonymous_variant | LOW | c.78C>T|p.His26His |
S167 |
7 | BAA05g31960 | A05 | 34369222 | C | T | upstream_gene_variant | MODIFIER | c.-1775G>A| |
S174 |
8 | BAA05g31960 | A05 | 34370595 | G | A | upstream_gene_variant | MODIFIER | c.-3148C>T| |
S65 |
9 | BAA05g31960 | A05 | 34370737 | C | T | upstream_gene_variant | MODIFIER | c.-3290G>A| |
S139 |
10 | BAA05g31960 | A05 | 34370989 | C | T | upstream_gene_variant | MODIFIER | c.-3542G>A| |
S251 |
11 | BAA05g31960 | A05 | 34371375 | C | T | upstream_gene_variant | MODIFIER | c.-3928G>A| |
S121 |
12 | BAA05g31960 | A05 | 34371617 | G | A | upstream_gene_variant | MODIFIER | c.-4170C>T| |
S76 |
13 | BAA05g31960 | A05 | 34371819 | C | T | upstream_gene_variant | MODIFIER | c.-4372G>A| |
S171 |